PlainRecalls
FDA Drug Moderate Class II Terminated

Famotodine Tablets, USP, 20 mg Tablets, For Repacking Only, Packaged in 6500 Count Drums, Over the Counter. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA. NDC: 64679-0374-09.

Reported: July 29, 2015 Initiated: April 22, 2015 #D-1266-2015

Product Description

Famotodine Tablets, USP, 20 mg Tablets, For Repacking Only, Packaged in 6500 Count Drums, Over the Counter. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA. NDC: 64679-0374-09.

Reason for Recall

CGMP Deviations: Firm did not adequately investigate customer complaints.

Details

Recalling Firm
Wockhardt Usa Inc.
Units Affected
539 Drums
Distribution
U.S. Nationwide including Puerto Rico.
Location
Parsippany, NJ

Frequently Asked Questions

What product was recalled?
Famotodine Tablets, USP, 20 mg Tablets, For Repacking Only, Packaged in 6500 Count Drums, Over the Counter. Manufactured by: Wockhardt Limited, Mumbai, India. Distributed by: Wockhardt USA LLC 20 Waterview Blvd. Parsippany, NJ 07054 USA. NDC: 64679-0374-09.. Recalled by Wockhardt Usa Inc.. Units affected: 539 Drums.
Why was this product recalled?
CGMP Deviations: Firm did not adequately investigate customer complaints.
Which agency issued this recall?
This recall was issued by the FDA Drug on July 29, 2015. Severity: Moderate. Recall number: D-1266-2015.